rs199473510

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs199473510(G;T)

Make rs199473510(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952616

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473510
dbSNP (classic)	rs199473510
ClinGen	rs199473510
ebi	rs199473510
HLI	rs199473510
Exac	rs199473510
Gnomad	rs199473510
Varsome	rs199473510
LitVar	rs199473510
Map	rs199473510
PheGenI	rs199473510
Biobank	rs199473510
1000 genomes	rs199473510
hgdp	rs199473510
ensembl	rs199473510
geneview	rs199473510
scholar	rs199473510
google	rs199473510
pharmgkb	rs199473510
gwascentral	rs199473510
openSNP	rs199473510
23andMe	rs199473510
SNPshot	rs199473510
SNPdbe	rs199473510
MSV3d	rs199473510
GWAS Ctlg	rs199473510

Max Magnitude

0

ClinVar
Risk	rs199473510(T;T)
Alt	rs199473510(T;T)
Reference	Rs199473510(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150649704C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057898.3,